Canonical Allele Identifier: CA2725175683
Gene: CBL HGNC NCBI

Linked Data

dbSNP Id: rs2135304013

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119278336A>C , CM000673.2:g.119278336A>C GRCh38
NC_000011.9:g.119149046A>C , CM000673.1:g.119149046A>C GRCh37
NC_000011.8:g.118654256A>C NCBI36
NG_016808.1:g.77057A>C , LRG_608:g.77057A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*679+39A>C ENSP00000515005.1:n.*679+39A>C
ENST00000264033.6:c.1227+39A>C MANE Select ENSP00000264033.3:n.1227+39A>C
ENST00000637974.1:c.1221+39A>C ENSP00000490763.1:n.1221+39A>C
ENST00000264033.5:c.1227+39A>C ENSP00000264033.3:n.1227+39A>C
ENST00000634586.1:c.1227+39A>C ENSP00000489218.1:n.1227+39A>C
ENST00000634840.1:c.1227+39A>C ENSP00000489324.1:n.1227+39A>C
NM_005188.3:c.1227+39A>C , LRG_608t1:c.1227+39A>C NP_005179.2:n.1227+39A>C
XM_011543057.1:c.1227+39A>C XP_011541359.1:n.1227+39A>C
NM_005188.4:c.1227+39A>C MANE Select NP_005179.2:n.1227+39A>C